Human SNP ID | rs1350666 |
---|---|
Human chromosome | chr4 |
Human SNP position | 74358873 |
Pig chromosome | chr8 |
Pig SNP position | 74496146 |
PubMed ID | 18821565 |
---|---|
Journal | Am J Med Genet B Neuropsychiatr Genet |
Link | www.ncbi.nlm.nih.gov/pubmed/18821565 |
Study | Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations. |
Disease/Trait | Attention deficit hyperactivity disorder |
Initial sample | 930 European ancestry trios |
Replication sample | NA |
Region | 4q13.3 |
Chromosome id | chr4 |
Chromosome position | 74358873 |
Reported gene | EREG |
Mapped gene | LOC105377276 - EREG |
Upstream gene id | 105377276 |
Downstream gene id | 2069 |
SNP gene ids | |
Upstream gene distance | 28557 |
Downstream gene distance | 6270 |
SNP risk allele | rs1350666-? |
SNPs | rs1350666 |
Merged | 0 |
SNP id current | 1350666 |
Context | intergenic_variant |
Intergenic | 1 |
Allele frequency | NR |
P value | 0.000008 |
Pvalue mlog | 5.09691001300805 |
P value text | (binary) |
Or beta | |
%95 Ci | |
Platform | Perlegen [429981] |
CNV | N |
Mapped trait | attention deficit hyperactivity disorder |
Mapped trait URI | http://www.ebi.ac.uk/efo/EFO_0003888 |
Study accession | GCST000281 |